High prevalence of anti-beta2 glycoprotein I antibodies in patients with ischemic heart disease

Autoimmunity. 1999;30(2):93-8. doi: 10.3109/08916939908994766.

Abstract

Ischemic cardiac manifestations have been reported in a various percentage of patients with anti-phospholipid antibodies. As concerns the relationship between anti-beta2 glycoprotein I antibodies (anti-beta2-GPI) and ischemic heart disease (IHD), it was investigated in only one coronary primary prevention study. We investigated the prevalence of anti-beta2-GPI in a well characterized group of patients with different clinical manifestation of IHD. Sera from 37 patients (mean age 62.7 +/- 9.9) with IHD (20 with unstable angina-UA and 17 with effort angina-EA) and from 40 healthy subjects, matched for age and sex, were tested for the presence of IgG and IgM anti-beta2-GPI using an ELISA technique. Eleven/37 patients (29.7%) resulted positive for anti-beta2-GPI. A positivity for IgG anti-beta2-GPI was found in 10 patients, 1 patient was positive for IgM and 1 for both isotypes. The prevalence of anti-beta2-GPI in the control group resulted significantly lower (2.5%; p < 0.005) than in patients with IHD. Positivity for anti-beta2-GPI was found in 9/20 (45%) patients with UA and only in 2/17 patients (11.8%) with EA (p = 0.0365). IgG anti-beta2-GPI levels (median 7.7U/ml, range 2.6-24.1) were significantly higher in patients with UA compared to patients with EA (median 4.6 U/ml, range 2.3-11.5; p = 0.02) and controls (median 3.15 U/ml, range 2.3-9.0; p < 0.0001); also IgM levels resulted higher in patients with unstable angina. A positivity for anti-beta2-GPI was observed in 4/13 patients (30.8%) with a previous myocardial infarction (MI) and in 7/24 (29.2%) patients without a previous MI. Our findings suggest that anti-beta2-GPI could represent an expression of the T-cell activation detectable in patients with unstable angina. The lack of a significant difference in the prevalence of these antibodies in patients with or without a previous MI suggests that anti-beta2-GPI are not induced by tissue necrosis.

Publication types

  • Comparative Study

MeSH terms

  • Aged
  • Angina Pectoris / blood
  • Angina Pectoris / immunology
  • Angina, Unstable / blood
  • Angina, Unstable / immunology*
  • Antibody Specificity
  • Antiphospholipid Syndrome / blood
  • Antiphospholipid Syndrome / immunology*
  • Antithrombin III / analysis
  • Autoantibodies / blood
  • Autoantibodies / immunology*
  • Autoimmune Diseases / blood
  • Autoimmune Diseases / immunology*
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Fibrin Fibrinogen Degradation Products / analysis
  • Glycoproteins / immunology*
  • Humans
  • Immunoglobulin M / immunology
  • Lymphocyte Activation
  • Male
  • Middle Aged
  • Myocardial Ischemia / epidemiology
  • Myocardial Ischemia / immunology
  • Peptide Fragments / analysis
  • Peptide Hydrolases / analysis
  • Prothrombin / analysis
  • Risk Factors
  • beta 2-Glycoprotein I

Substances

  • Autoantibodies
  • Fibrin Fibrinogen Degradation Products
  • Glycoproteins
  • Immunoglobulin M
  • Peptide Fragments
  • antithrombin III-protease complex
  • beta 2-Glycoprotein I
  • fibrin fragment D
  • prothrombin fragment 1.2
  • Antithrombin III
  • Prothrombin
  • Peptide Hydrolases